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Neonatal DEX exposure leads to hyperanxious and depressive-like behaviors as well as a persistent reduction of BDNF expression in developmental stages

机译:新生儿DEX暴露导致沉重和抑郁的行为,以及在发育阶段的BDNF表达持续减少

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摘要

Brain-derived neurotrophic factor (BDNF), which regulates the neuronal survival, differentiation and synaptic plasticity, has been proved to play a critical role in the pathology and treatment of several psychiatric disorders including depression. Dexamethaone (DEX) is indicated for a number of conditions in perinatal medicine, however, the long-term impact of early-life DEX exposure on BDNF expression in hippocampus remains unknown. Here we found that neonatal DEX(ND) exposure leads to insignificant change of BDNF expression levels in the adulthood, albeit increased hyperanxious and depressive-like behaviors. However, the bdnf mRNA and BDNF protein levels were significantly reduced in all the hippocampal subregions during the developmental stages, including the perinatal period and puberty. We conclude that early life DEX exposure leads to a persistent disturbance of BDNF signaling during the developmental stages, which might be associated with the life-long impairment of hippocampal function. (C) 2020 Elsevier Inc. All rights reserved.
机译:已经证明,调节神经元存活,分化和突触可塑性的脑衍生的神经营养因子(BDNF)在病理和治疗包括抑郁症,包括抑郁症的病理和治疗中起着关键作用。目单地(DEX)在围产药中表明了许多条件,然而,早期DEX暴露对海马BDNF表达的长期影响仍然未知。在这里,我们发现新生儿DEX(ND)曝光导致成年期的BDNF表达水平的不显着变化,尽管增加过血糖和抑郁的行为。然而,在发育阶段的所有海马次区域中,BDNF mRNA和BDNF蛋白水平显着降低,包括围产期和青春期。我们得出结论,早期寿命DEX暴露导致在发育阶段期间BDNF信号传导的持续扰动,这可能与海马功能的终身损害有关。 (c)2020 Elsevier Inc.保留所有权利。

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